Drug metabolism in the lungs: opportunities for optimising inhaled medicines

被引:34
|
作者
Enlo-Scott, Zachary [1 ]
Backstrom, Erica [2 ]
Mudway, Ian [3 ,4 ,5 ]
Forbes, Ben [1 ]
机构
[1] Kings Coll London, Fac Life Sci & Med, Inst Pharmaceut Sci, London, England
[2] AstraZeneca, Drug Metab & Pharmacokinet, Res & Early Dev, Resp & Immunol R&I,BioPharmaceut R&D, Gothenburg, Sweden
[3] Imperial Coll London, MRC Ctr Environm & Hlth, Sch Populat Hlth & Environm Sci, London, England
[4] Imperial Coll London, Natl Inst Hlth Res, Hlth Protect Res Unit Chem & Radiat Threats & Haz, London, England
[5] Imperial Coll London, Natl Inst Hlth Res, Hlth Protect Res Unit Environm Exposures & Hlth, London, England
关键词
Respiratory; pulmonary; drug metabolism; lung metabolism; inhaled drugs; pharmacokinetics; inhalation toxicology; pro-drug; soft drug; FLUTICASONE PROPIONATE; PROTEASE INHIBITORS; PULMONARY; EXPRESSION; PHARMACOKINETICS; CICLESONIDE; ROFLUMILAST; ABSORPTION; CALCITONIN; DELIVERY;
D O I
10.1080/17425255.2021.1908262
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction The lungs possess many xenobiotic metabolizing enzymes which influence the pharmacokinetics and safety of inhaled medicines. Anticipating metabolism in the lungs provides an opportunity to optimize new inhaled medicines and overcome challenges in their development. Areas covered This article summarizes current knowledge on xenobiotic metabolizing enzymes in the lungs. The impact of metabolism on inhaled medicines is considered with examples of how this impacts small molecules, biologics and macromolecular formulation excipients. Methods for measuring and predicting xenobiotic lung metabolism are critically reviewed and the potential for metabolism to influence inhalation toxicology is acknowledged. Expert opinion Drugs can be optimized by molecular modification to (i) reduce systemic exposure using a 'soft drug' approach, (ii) improve bioavailability by resisting metabolism, or (iii) use a prodrug approach to overcome pharmacokinetic limitations. Drugs that are very labile in the lungs may require a protective formulation. Some drug carriers being investigated for PK-modification rely on lung enzymes to trigger drug release or biodegrade. Lung enzyme activity varies with age, race, smoking status, diet, drug exposure and preexisting lung disease. New experimental technologies to study lung metabolism include tissue engineered models, improved analytical capability and in silico models.
引用
收藏
页码:611 / 625
页数:15
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